Kubtec DIGIVIEW 395— 510(k) K151221
Substantially EquivalentKub Technologies, Inc.
FDA 510(k) clearance K151221 for Kubtec DIGIVIEW 395, Substantially Equivalent on 2015-06-23. Applicant: Kub Technologies, Inc.. Device class: 2.
Clearance details
- Applicant
- Kub Technologies, Inc.
- Product code
- Code MQB
- Device class
- Class 2
- Regulation
- 21 CFR 892.1680
- Advisory panel
- Radiology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Milford, CT, US
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